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Comment: Comment: BCR/TCR analysis using target capture sequencing data
11 months ago by J.F.Jiang ▴ 920
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1
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952
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Comment: Comment: combine/merge closet variants into one from mutect2
11 months ago by J.F.Jiang ▴ 920
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1
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952
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Comment: Comment: combine/merge closet variants into one from mutect2
11 months ago by J.F.Jiang ▴ 920
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1
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709
views
Comment: Comment: BCL2 fusions not detected in RNA level
12 months ago by J.F.Jiang ▴ 920
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1
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903
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Comment: Comment: tumor fraction estimation for ctDNA panel sequecing data
2.1 years ago by J.F.Jiang ▴ 920
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0
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996
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Comment: C: public tools to distinguish germline variants from somatic ones in NGS data with
3.4 years ago by J.F.Jiang ▴ 920
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1
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996
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Comment: C: public tools to distinguish germline variants from somatic ones in NGS data with
3.4 years ago by J.F.Jiang ▴ 920
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1
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968
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Comment: C: HPV EBV typing from cancer genome data
3.7 years ago by J.F.Jiang ▴ 920
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1
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2.2k
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Comment: C: fusion detection for DNA Sequencing data
4.1 years ago by J.F.Jiang ▴ 920
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0
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2.2k
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Comment: C: fusion detection for DNA Sequencing data
4.1 years ago by J.F.Jiang ▴ 920
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0
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1.5k
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Comment: C: CNV analysis for tumor panel
4.1 years ago by J.F.Jiang ▴ 920
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0
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994
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Comment: C: convenient tools to collect target mapping metrics
4.4 years ago by J.F.Jiang ▴ 920
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1
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23k
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Comment: C: Bwa Mem Method For Mapping, With Or Without Trimming Reads?
updated 4.6 years ago by 43k • written 10.3 years ago by ▴ 920
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1
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1.5k
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Comment: A: CNV analysis for tumor panel
4.8 years ago by J.F.Jiang ▴ 920
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0
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2.6k
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Comment: C: Free Genetic Genealogy Software
5.7 years ago by J.F.Jiang ▴ 920
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0
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2.7k
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Comment: C: remove primer sequences from BAM file
5.7 years ago by J.F.Jiang ▴ 920
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1
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2.7k
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Comment: C: remove primer sequences from BAM file
updated 5.7 years ago by 47k • written 5.7 years ago by ▴ 920
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0
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1.7k
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Comment: C: extract region bam
6.4 years ago by J.F.Jiang ▴ 920
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0
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1.4k
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Comment: C: pairwise calculation of relationship based on selected SNPs with MAF>0.3
6.4 years ago by J.F.Jiang ▴ 920
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0
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8.5k
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Comment: C: GATK HaolotypeCaller takes too much time for variant calling
6.5 years ago by J.F.Jiang ▴ 920
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1
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1.5k
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Comment: C: Fasted method to genotype given SNPs from NGS data
6.5 years ago by J.F.Jiang ▴ 920
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1
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8.5k
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Comment: C: GATK HaolotypeCaller takes too much time for variant calling
6.5 years ago by J.F.Jiang ▴ 920
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0
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1.4k
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Comment: C: allelic unbalance for multiplex PCR based amplicon data
6.6 years ago by J.F.Jiang ▴ 920
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0
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1.4k
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Comment: C: allelic unbalance for multiplex PCR based amplicon data
6.6 years ago by J.F.Jiang ▴ 920
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0
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2.9k
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Comment: C: amplicon based germline CNV caller
6.6 years ago by J.F.Jiang ▴ 920
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0
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2.9k
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Comment: C: amplicon based germline CNV caller
6.7 years ago by J.F.Jiang ▴ 920
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0
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3.5k
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Comment: C: any tools to get clean reads for illumina reads
6.7 years ago by J.F.Jiang ▴ 920
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0
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3.5k
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Comment: C: any tools to get clean reads for illumina reads
6.7 years ago by J.F.Jiang ▴ 920
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1
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3.5k
views
Comment: C: any tools to get clean reads for illumina reads
6.7 years ago by J.F.Jiang ▴ 920
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0
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1.3k
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Comment: C: variant calling discondordance between same sample between two run
6.8 years ago by J.F.Jiang ▴ 920
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1
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1.8k
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Comment: C: CYP2D6 alleles determination
8.4 years ago by J.F.Jiang ▴ 920
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1
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3.8k
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Comment: C: primer design using BLASTn
8.5 years ago by J.F.Jiang ▴ 920
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0
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3.5k
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Comment: C: obtain a simulated bam file for variants on existed bam file
8.6 years ago by J.F.Jiang ▴ 920
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1
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3.5k
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Comment: C: obtain a simulated bam file for variants on existed bam file
8.6 years ago by J.F.Jiang ▴ 920
1
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0
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18k
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Comment: C: How To Plot Clustered Mutation Profiles Using Tcga Mutation Data
9.2 years ago by J.F.Jiang ▴ 920
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0
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2.4k
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Comment: Comment: database of genetic alternations for inherited cancer
updated 2.1 years ago by 43k • written 9.3 years ago by ▴ 920
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0
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2.4k
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Comment: Comment: database of genetic alternations for inherited cancer
updated 2.1 years ago by 43k • written 9.3 years ago by ▴ 920
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0
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3.2k
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Comment: Comment: primer design function for perl program
updated 2.1 years ago by 43k • written 9.3 years ago by ▴ 920
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0
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3.2k
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Comment: Comment: primer design function for perl program
updated 2.1 years ago by 43k • written 9.3 years ago by ▴ 920
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0
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3.2k
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Comment: C: Multiple tissue eQTL list
9.3 years ago by J.F.Jiang ▴ 920
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2
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3.2k
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Comment: Comment: Multiple tissue eQTL list
updated 2.2 years ago by 43k • written 9.4 years ago by ▴ 920
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0
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2.3k
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Comment: Comment: marker information for cancer that have been accessed by FDA
updated 2.2 years ago by 43k • written 9.4 years ago by ▴ 920
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1
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4.4k
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Comment: Comment: CNV frequency database for review
updated 2.2 years ago by 43k • written 9.5 years ago by ▴ 920
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0
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17k
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Comment: Comment: disadvantage of NextSeq 500 compared with MiSeq
updated 2.2 years ago by 43k • written 9.5 years ago by ▴ 920
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0
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17k
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Comment: C: disadvantage of NextSeq 500 compared with MiSeq
9.5 years ago by J.F.Jiang ▴ 920
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0
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2.7k
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Comment: C: get genebank information based on NM accession ID
9.6 years ago by J.F.Jiang ▴ 920
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0
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3.4k
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Comment: C: Automatic clustering for gene expressing matrix
9.6 years ago by J.F.Jiang ▴ 920
1
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0
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3.4k
views
Comment: Comment: Automatic clustering for gene expressing matrix
updated 2.3 years ago by 43k • written 9.6 years ago by ▴ 920
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1
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3.4k
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Comment: C: Automatic clustering for gene expressing matrix
9.6 years ago by J.F.Jiang ▴ 920
0
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0
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6.7k
views
Comment: Comment: parameter in blastn to limit the output to top 20 best hits
updated 2.3 years ago by 43k • written 9.6 years ago by ▴ 920
149 results • Page 1 of 3
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